共查询到19条相似文献，搜索用时 109 毫秒
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运用已建立的气溶胶核化清除的物理化学模式，研究了云的动力学因子（如:气块上升速度、夹卷作用）对云滴化学非均匀性的影响。计算结果表明:较强烈的云发展（较大的气块上升速度）可加强由于气溶胶核化和云滴凝结增长造成的云滴化学的非均匀程度。夹卷作用抑制了云的发展，因而减弱了这种非均匀程度。夹卷作用同时也造成总体液态水中S(VI)、Ｈ+等浓度的增加，在Ｓｍａｘ附近可达１个量级。如果考虑气溶胶粒子的夹卷，则可使气块内云滴污染物浓度随云滴大小的变化更加复杂化，如:不仅云滴污染物浓度随云滴大小而变化，即使对于相同大小的云滴之间，其污染物浓度也可相差很大。 相似文献
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运用已建立的气溶胶核化清除的物理化学模式，研究了云的动力学因子（如：气块上升速度、夹卷作用）对云滴化学非均匀性的影响。计算结果表明：较强烈的云发展（较大的气块上升速度）可加强由于气溶胶核化和云滴凝结增长造成的云滴化学的非均匀程度。夹卷作用抑制了云的发展，因而减弱了这种非均匀程度。夹卷作用同时也造成总体液态水中Ｓ（ＶＩ）、Ｈ＋等浓度的增加，在Ｓｍａｘ附近可达１个量级。如果考虑气溶胶粒子的夹卷，则可使气块内云滴污染物浓度随云滴大小的变化更加复杂化，如：不仅云滴污染物浓度随云滴大小而变化，即使对于相同大小的云滴之间，其污染物浓度也可相差很大。 相似文献
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云化学模式及其若干研究进展 总被引：1，自引：0，他引：1
本文从云的微物理过程、云中化学反应、云水、雨水对污染气体和气溶胶的清除过程,云化学模式等方面,总结介绍了近几年来云化学模式的若干研究进展。 相似文献
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气溶胶的时空分布及其核化成云的转化过程是云降水物理研究的重点,也是气候变化中气溶胶间接效应关注的热点问题。利用2013～2014年期间在华北中部山西地区开展的9架次夏季晴天和积云天气情况下的气溶胶、云凝结核（CCN）及云滴数浓度观测资料,分析研究了气溶胶的垂直分布、谱分布、来源特征及其与云凝结核、云滴数浓度的转化关系。研究结果表明,大气边界层逆温层结对气溶胶、CCN垂直分布有重要影响,不同天气条件下气溶胶谱型在低层差异较大而高层基本一致;垂直方向上CCN数浓度与气溶胶数浓度有较好的相关性,过饱和度0.3%条件下CCN比率（云凝结核/凝结核）与气溶胶有效直径呈线性关系;积云云下气溶胶与云滴的线性拟合方程为y=1.3x?616.3,拟合相关系数为0.96,气溶胶转化为云滴的比率可达到47%。在过饱和度0.3%条件下,云下CCN与云滴的线性拟合方程为y=1.6x?473.8,拟合相关系数也为0.96,CCN转化为云滴的比率可达到69%。 相似文献
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云滴谱宽度对模式中云的光学厚度的参数化、气溶胶间接效应的评估以及降水形成过程的研究至关重要。本文利用美国POST（Physics of Stratocumulus Top）项目2008年7月19日的飞机观测资料，分析了微物理量和云滴谱的垂直分布及微物理过程。结果表明，该云系云滴谱宽度在云底附近较大，这是由低层核化过程导致的；中层凝结增长过程使得云滴谱宽度随高度增加逐渐减小；云顶附近夹卷混合过程导致云滴谱宽度增大。绝热云中垂直速度的增大会促进云凝结核的活化使云滴数浓度增大，促进凝结增长使云滴尺度增大、云滴谱宽度减小，云滴谱宽度与云滴数浓度、云滴尺度呈现负相关关系；云洞中受夹卷混合过程影响，垂直速度减小，云滴蒸发，云滴数浓度和云滴尺度减小、云滴谱宽度增大，且该效应随绝热程度减小而增强。建议云滴谱宽度的参数化将垂直速度、云滴数浓度、云滴尺度和绝热程度等考虑在内。 相似文献
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在UWyo单组分气溶胶的绝热气块分档云模式基础上,发展了多种化学组分气溶胶的绝热气块分档云模式。利用2006年春季华北地区地面气溶胶分级采样的离子成分分析数据和同时段高空气溶胶、云微物理飞机观测资料,研究了气溶胶混合状态对暖云微物理特征的影响。模拟结果表明,华北地区气溶胶内部混合比外部混合有利于增加云凝结核数浓度、降低气块水汽最大饱和比、增加云滴数浓度。气溶胶的混合状态不同,形成的云滴谱的特征差异较大,主要体现在云滴谱的平均尺度和峰值的突出程度;云滴谱相对离散度在0.3附近变化,且随着云滴数浓度的增加,云滴谱相对离散度呈现减小的趋势。气溶胶混合状态能够影响暖云微物理特征,从而影响大气辐射和降水过程,在天气和气候变化的研究中应予以关注。 相似文献
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A one-dimensional cumulus cloud chemistry model(1CCCM)is developed to simulate cloudphysical processes and chemical processes during the evolution of a convective cloud.The cloudphysical submodel includes a detailed microphysical parameterized scheme of 20 processes.Thechemistry submodel is composed of three parts:gas phase chemistry,aqueous phase chemistry andscavenging of soluble gases.The gas phase reaction mechanism contains 85 reactions among 45species including 13 organics.The aqueous phase reaction mechanism contains 54 reactions among40 species and 12 ion equilibria.Mass of 19 gases is transported between the gas phase and theaqueous phase.With this model,studies may be made to analyze the interactions among processesduring lifetime of a cumulus cloud. 相似文献
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A one-dimensional cumulus cloud chemistry model(ICCCM) is developed to simulate cloud physical processes and chemical processes during the evolution of a convective cloud.The cloud physical submodel includes a detailed microphysical parameterized scheme of 20 processes.The chemistry submodel is composed of three parts:gas phase chemistry,aqueous phase chemistry and scavenging of soluble gases.The gas phase reaction mechanism contains 85 reactions among 45 species including 13 organics.The aqueous phase reaction mechanism contains 54 reactions among 40 species and 12 ion equilibria.Mass of 19 gases is transported between the gas phase and the aqueous phase.With this model,studies may be made to analyze the interactions among processes during lifetime of a cumulus cloud. 相似文献
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云对云中大气臭氧影响因子的分析 总被引：3，自引：0，他引：3
应用一个较详细的气相光化学和液相化学耦合的箱体模式, 研究了云层对云中大气臭氧的影响过程。这一过程可分解为三个因子来考虑： 因子Ａ （云的辐射效应）, 由于云的存在改变太阳光辐射通量, 使得对流层光化学反应减弱或增强, 从而降低或增加臭氧浓度; 因子Ｂ（云的吸收效应）, 云层中液态水对大气臭氧及其前体物 （ＮＯｘ、ＮＭＨＣ、自由基等） 的直接吸收作用; 因子Ｃ（云的液相化学效应）, 吸收进入云中的物质发生液相化学反应从而改变大气臭氧浓度。数值研究结果表明： 上述三因子对云中臭氧浓度影响的程度差别很大, 并且与云层的物理结构有密切关系。讨论了云的吸收及液相化学效应影响臭氧浓度的主要原因 相似文献
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A chemistry module has been incorporated into a Lagrangian type model that computes the dynamics and microphysics of an orographical cloud formed in moist air flowing over the summit of Great Dun Fell (GDF) in England. The cloud droplets grow on a maritime aerosol which is assumed to be an external mixture of sea-salt particles and ammonium-sulfate particles. The dry particle radii are in the range 10 nm<r<1 µm. The gas-phase chemical reaction scheme considers reactions of nitrogen compounds that are important at night. The treatment of scavenging of gases into the aqueous phase in the model takes into account the different solubilities and accommodation coefficients. The chemistry in the aqueous phase focusses on the oxidation of S(IV) via different pathways.Sensitivity analyses have been performed to investigate deviations from gas-liquid equilibria according to Henry's law and also to study the influence of iron and of nitrogen compounds on the aqueous-phase oxidation of dissolved SO2. When addressing these questions, special attention has been given to the dependence on the droplet size distribution and on the chemical composition of the cloud condensation nuclei on which the droplets have formed. It was found that the oxidation of S(IV) via a chain reaction of sulfur radicals can be important under conditions where H2O2 is low. However, major uncertainties remain with respect to the interaction of iron with the radical chain. It was shown that mixing of individual cloud droplets, which are not in equilibrium according to Henry's law, can result in a bulk sample in equilibrium with the ambient air. The dependence of the aqueous-phase concentrations on the size of the cloud droplets is discussed for iron, chloride and NO3. 相似文献
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沙尘气溶胶粒子表面变性对云滴形成过程的影响 总被引：9，自引：2，他引：9
利用1997年5月14日辽宁省气溶胶和云滴谱航测资料,讨论了沙尘气溶胶粒子表面变性产生的不溶性沙尘粒子外包可溶性硫酸铵层的混合气溶胶粒子作为凝结核的增长规律,计算了由混和核形成的云滴谱特征,并与纯硫酸铵盐核进行对比.结果表明:混和核上初期形成的云滴谱型比纯硫酸铵盐核上初期形成的云滴谱型要宽,更接近实际观测到的云滴谱分布. 相似文献
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Maud Leriche R. Lyana Curier Laurent Deguillaume Dimitri Caro Karine Sellegri Nadine Chaumerliac 《Journal of Atmospheric Chemistry》2007,57(3):281-297
The Model of Multiphase Cloud Chemistry M2C2 has recently been extended to account for nucleation scavenging of aerosol particles in the cloud water chemical composition. This extended version has been applied to multiphase measurements available at the Puy de Dôme station for typical wintertime anthropogenic air masses. The simulated ion concentrations in cloud water are in reasonable agreement with the experimental data. The analysis of the sources of the chemical species in cloud water shows an important contribution from nucleation scavenging of particles which prevails for nitrate, sulphate and ammonium. Moreover, the simulation shows that iron, which comes only from the dissolution of aerosol particles in cloud water, has a significant contribution in the hydroxyl radical production. Finally, the simulated phase partitioning of chemical species in cloud are compared with measurements. Numerical results show an underestimation of interstitial particulate phase fraction with respect to the measurements, which could be due to an overestimation of activated mass by the model. However, the simulated number scavenging efficiency of particles agrees well with the measured value of 40% of total number of aerosol particles activated in cloud droplets. Concerning the origin of chemical species in cloud water, the model reproduces quite well the contribution of gas and aerosol scavenging estimated from measurements. In addition, the simulation provides the contribution of in-cloud chemical reactivity to cloud water concentrations. 相似文献
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积云对二氧化硫和硫酸盐气溶胶作用的研究 总被引：1，自引：1，他引：0
利用一个冰雹云模式与云化学模式耦合而成的二维积云化学模式,研究对流云的输送、微物理转化、云内化学过程、湿清除对SO2及硫酸盐气溶胶的作用。云化学模式的结果表明,由于SO2在向上输送的过程中可溶解于云水和雨水中,从而阻止了SO2向上部的转移,因此对气相SO2来说,云的输送是一个相当无效的过程,而液相清除起主要作用。硫酸盐气溶胶的收支分析表明,降水清除了1.67 mol的SO2-4,占气溶胶总量的64%,其中液态降水清除了0.72 mol,固态降水清除了0.95 mol,说明了冰相过程在硫沉降中的重要性。 相似文献
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R. N. Colvile R. Sander T. W. Choularton K. N. Bower D. W. F. Inglis W. Wobrock D. Schell I. B. Svenningsson A. Wiedensohler H. -C. Hansson A. Hallberg J. A. Ogren K. J. Noone M. C. Facchini S. Fuzzi G. Orsi B. G. Arends W. Winiwarter T. Schneider A. Berner 《Journal of Atmospheric Chemistry》1994,19(1-2):189-229
The airflow, cloud microphysics and gas- and aqueous-phase chemistry on Kleiner Feldberg have been modelled for the case study of the evening of 1 November 1990, in order to calculate parameters that are not easily measured in the cloud and thus to aid the interpretation of the GCE experimental data-set. An airflow model has been used to produce the updraught over complex terrain for the cloud model, with some care required to ensure realistic modelling of the strong stable stratification of the atmosphere. An extensive set of measurements has been made self-consistent and used to calculate gas and aerosol input parameters for the model. A typical run of the cloud model has calculated a peak supersaturation of 0.55% which occurs about 20 s after entering cloud where the updraught is 0.6 m s–1. This figure has been used to calculate the efficiency with which aerosol particles were scavenged; it is higher than that calculated by other methods, and produces a cloud with slightly too many droplets. A broad cloud droplet size spectrum has been produced by varying the model inputs to simulate turbulent mixing and fluctuations in cloud parameters in space and time, and the ability of mixing processes near cloud-base to produce a lower peak supersaturation is discussed. The scavenging of soluble gases by cloud droplets has been observed and departures from Henry's Law in bulk cloud-water samples seen to be caused by variation of pH across the droplet spectrum and the inability of diffusion to adjust initial distributions of highly soluble substances across the spectrum in the time available. Aqueous-phase chemistry has been found to play a minor role in the cloud as modelled, but circumstances in which these processes would be more important are identified. 相似文献
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Randolph D. Borys Edward E. Hindman Paul J. DeMott 《Journal of Atmospheric Chemistry》1988,7(3):213-239
The relationships between the physical and chemical properties of mixed-phase clouds were investigated at Storm Peak Laboratory (3220m MSL) located near the continental divide in northwestern Colorado. Interstitial aerosol particles, cloud droplets and snow crystals were concurrently collected when the laboratory was enveloped by a precipitating cloud. All samples were analyzed for trace elements, soluble anions, electrical conductivity and acidity.The results show average trace constituent concentration ratios of cloud water to snow water range from 0.4 to 26. All but six of the 32 elements and ions measured had ratios greater than one. This result suggests a chemical species dependency of in-cloud aerosol particle scavenging processes. Evidence of a decrease of in-cloud aerosol particle scavenging efficiency by snow due to increases in aerosol concentration is also presented.Differences between the chemical composition of cloud water and snow water are manifested most strongly when snow crystals grow by vapor deposition. In-cloud scavenging efficiencies by snow crystals for most aerosol particle chemical species are dependent on the growth of the snow crystals by accretion of cloud droplets. This chemical fractionation of the atmospheric aerosol by snow crystal formation and growth should be most active where narrow, continental cloud droplet size distributions and low liquid water contents are prevalent, enhancing the probability of snow crystal growth by diffusion. 相似文献